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Research Article

Molecular genetic variation in the East Midlands, England: analysis of VNTR, STR and Alu insertion/deletion polymorphisms

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Pages 538-550 | Published online: 09 Jul 2009

References

  • BATZER, M. A., ARCOT, S. S., PHINNEY, J. W., ALEGRIA-HARTMAN, M., KASS, D. H., MILLIGAN, S. M., KIMPTON, C., GILL, P., HOCHMEISTER, M., IOANNOU, P. A., HERRERA, R. J., BOUDREAU, D. A., SCHEER, W. D., KEATS, B. J., DEININGER, P. L., and STONEKING, M., 1996, Genetic variation of recent Alu insertions in human populations. Journal of Molecular Evolution, 42, 22–29.
  • BRINKMANN, B., JUNGE, A., MEYER, E., and WIEGAND, P., 1998, Population genetic diversity in relation to microsatellite heterogeneity. Human Mutation, 11, 135–144.
  • BUDOWLE, B., and MONSON, K. L., 1994, Greater differences in forensic DNA profile frequencies estimated from racial groups than from ethnic subgroups. Clinca Chimca Acta, 228, 3–18.
  • BUDOWLE, B., CHAKRABORTY, R., GUISTI, A. M., EISENBERG, A. J., and ALLEN, R. C., 1991a, Analysis of the VNTR locus D1S80 by the PCR following high-resolution PAGE. American Journal of Human Genetics, 48, 137–144.
  • BUDOWLE, B., GIUSTI, A. M., WAYE, J. S., BAECHTEL, F. S., FOURNEY, R. M., ADAMS, D. E., PRESLEY, L. A., DEADMAN, H. A., and MONSON, K. L., 1991b, Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons. American Journal of Human Genetics, 48, 841–855.
  • DEKA, R., SHRIVER, M. D., Yu, L. M., FERRELL, R. E., and CHAKRABORTY, R., 1995, Intra- and inter-population diversity at short tandem repeat loci in diverse populations of the world. Electrophoresis, 16, 1659–1664.
  • GILL, P., and EVETT, I. W., 1995, Population genetics of short tandem (STR) loci. Genetica, 96, 69–87.
  • GREENACRE, M. J., 1984, Theory and Applications of Correspondence Analysis (New York: Academic Press).
  • HIORNS, R. W., HARRISON, G. A., and GIBSON, J. B., 1977, Genetic variation in some Oxfordshire villages. Annals of Human Biology, 4, 197–210.
  • LANCHBURY, J. S., PAPIHA, S. S., and ROBERTS, D. F., 1990, Genetic variation in north-east England. Annals of Human Biology, 17, 265–276.
  • MARTINOVIC, I., MASTANA, S., JANICUEVIC, B., JOVANOVIC, V., PAPHIA, S. S., ROBERTS, D. F., and RUDAN, P., 1998, VNTR DNA variation in the population of the island of Hvar, Croatia. Annals of Human Biology, 25, 489–499.
  • MASTANA, S. S., and PAPIHA, S. S., 2001, D1S80 distribution in world populations with new data from the UK and the Indian sub-continent. Annals of Human Biology, 28, 308–318.
  • MASTANA, S. S., and SINGH, P. P., 2002, Population genetic study of the STR loci (HUMCSF1P0, HUMTPDX, HUMTH01, HUMLPL, HUMF13A01, HUMF13B, HSFESFPS, and HUMVWA) in North Indians. Annals of Human Biology, 29, 677–684.
  • MASTANA, S. S., and SoKoL, R. J., 1998, Genetic variation in the East Midlands. Annals of Human Biology, 25, 43–68.
  • MITCHELL, R. J., IZATT, M. M., SUNDERLAND, E., and CARTWRIGHT, R. A., 1976, Blood groups antigens, plasma protein and red cell isoenzyme polymorphisms in south-west Scotland. Annals of Human Biology, 3, 57–71.
  • NEI, M., TAJIMA, F., and TATENO, Y., 1983, Accuracy of estimated phylogenetic trees from molecular data. II. Gene frequency data. Journal of Molecular Evolution, 19, 153–170.
  • PAPIHA, S. S., MASTANA, S. S., PURANDARE, C. A., JAYASEKARA, R., and CHAKRABORTY, R., 1996, A population genetic study of three VNTR loci (D2S44, D7S22, D12 S11) in five ethnically defined populations of Indian Subcontinent. Human Biology, 68, 819–835.
  • PAPIHA, S. S., CALDERON, R., SERTEDAKI, A., PENA, J., ZHONG, Y., and CHAKRABORTY, R., 1998, Study of three hypervariable DNA loci (D1S7, D7S22 and D12S11) in three European populations. Annals of Human Biology, 25, 29–41.
  • PEREZ-LEZAUN, A., CALAFELL, F., MATEU, E., COMAS, D., BOSCH, E., and BERTRANPETIT, J., 1997, Allele frequencies for 20 microsatellites in a worldwide population survey. Human Heredity, 47, 189–196.
  • ROBERTS, D. F., 1973, The origins of genetic variation in Britain. In Genetic Variation in Britain, edited by D. F. Roberts and E. Sunderland (London: Taylor & Francis), pp. 1–16.
  • ROBERTS, D. F., JORDE, L. B., and MITCHELL, R. J., 1981a, Genetic structure in Cumbria. Journal of Biosocial Science, 13, 317–336.
  • ROBERTS, D. F., MITCHELL, R. J., CREEN, C. K., and JORDE, L. B., 1981b, Genetic variation in Cumbrians. Annals of Human Biology, 8, 135–144.
  • STONEKING, M., FONTIUS, J. J., CLIFFORD, S. L., SOODYALL, H., ARCOT, S. S., SAHA, N., JENKINS, T., TAHIR, M. A., DEININGER, P. L., and BATZER, M. A., 1997, Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Research, 7, 1061–1071.
  • THOMSON, J. A., PILOTTI, V., STEVENS, P., AYRES, K. L., and DEBENHAM, P. G., 1999, Validation of short tandem repeat analysis for the investigation of cases of disputed paternity. Forensic Science International, 100, 1–16.
  • WEALE, M. E., WEISS, D. A., JAGER, R. F., BRADMAN, N., and THOMAS, M. G., 2002, Y chromosome evidence for Anglo-Saxon mass migration. Molecular Biology and Evolution, 19, 1008–1021.
  • WILSON, J. F., WEISS, D. A., RICHARDS, M., THOMAS, M. G., BRADMAN, N., and GOLDSTEIN, D. B., 2001, Genetic evidence for different male and female roles during cultural transitions in the British Isles. Proceedings of the National Academy of Sciences USA, 98, 5078–5083.

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